Prophylactic Treatment With Atorvastatin for Chronic Migraine (ChronicStatinMig)
ChronicStatinMig. A Multicentre, Triple Blind, Placebo Controlled, Parallel Group Study of Atorvastatin in Chronic Migraine
1 other identifier
interventional
300
1 country
6
Brief Summary
The main objective of this study is to see whether the favorable preventative effect of Atorvastatin 40mg per day in episodic migraine, that was found previously in three smaller randomized controlled cross-over studies, can be confirmed in a larger, multicenter, randomized controlled parallel group study. In addition it will be investigated whether 1) the favorable side effect profile, seen in previous studies, can be confirmed, and whether it is even better with the smaller dose, and 2) estimating the cost of Atorvastatin treatment, considering cost of medicine, cost of acute attack medicine, and cost of lost worktime.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Started May 2024
Longer than P75 for phase_2
6 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2024
CompletedFirst Submitted
Initial submission to the registry
June 10, 2024
CompletedFirst Posted
Study publicly available on registry
July 3, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 28, 2029
July 1, 2025
June 1, 2025
4.7 years
June 10, 2024
June 29, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of migraine days
Change in number of migraine days/4 weeks from the baseline period to the intervention period.
4 weeks
Secondary Outcomes (4)
Number of responders
12 weeks
Rate of adverse events
12 weeks
Number of doses with acute medication
12 weeks
Number of days with sick leave
12 weeks
Study Arms (2)
Atorvastatin 40mg
ACTIVE COMPARATOREach participant in this arm will receive 40mg atorvastatin once daily for 84 days.
Placebo
PLACEBO COMPARATOREach participant in this arm will receive placebo once daily for 84 days.
Interventions
Each tablet will be taken once daily for 84 days.
Eligibility Criteria
You may qualify if:
- Age 18 to 64 years
- Signed informed consent
- Chronic migraine according to ICHD-3 criteria (32)
- Start of migraine before age 50 years.
- No use of other migraine prophylactics during the study
- For women of child-bearing potential (WOCBP, see below) there must be no pregnancy or planned pregnancy during the study period, and use of highly effective contraception (See below).
You may not qualify if:
- Medication overuse headache requiring detoxification from acute medication (triptans, opioids). Exception could be made for those fulfilling A and B:
- A. Have tried a withdrawal period of at least 2 months without impact on headache frequency B: Use of opioids (of any type) ≤ 8 days /months.
- Clinical information on or signs of cholestasis or decreased hepatic or renal function.
- High degree of comorbidity and/or frailty associated with reduced life expectancy or high likelihood of hospitalization, at the discretion of the investigator
- Hypersensitivity to statins or previous use of statins
- History of angioneurotic oedema
- Use of medicines for migraine prophylaxis less than 4 weeks, or of botulinum toxin less than 16 weeks, prior to start of study
- Current use of antiviral treatment agaist hepatitis C
- Significant psychiatric illness
- Alcohol or illicit drug dependence.
- Inability to understand study procedures and to comply with them for the entire length of the study
- Treatment for hypothyroidism
- Lactose intolerance
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- St. Olavs Hospitallead
- Haukeland University Hospitalcollaborator
- Oslo University Hospitalcollaborator
- University Hospital of North Norwaycollaborator
- University Hospital, Akershuscollaborator
- Ullevaal University Hospitalcollaborator
Study Sites (6)
Haukeland University Hospital
Bergen, Norway
University Hospital, Akershus
Lørenskog, Norway
Oslo University Hospital, Rikshospitalet
Oslo, Norway
Oslo University Hospital, UllevĂ¥l
Oslo, Norway
University Hospital Northern Norway
Tromsø, Norway
St. Olavs hospital
Trondheim, Norway
Related Publications (31)
Steiner TJ, Stovner LJ, Jensen R, Uluduz D, Katsarava Z; Lifting The Burden: the Global Campaign against Headache. Migraine remains second among the world's causes of disability, and first among young women: findings from GBD2019. J Headache Pain. 2020 Dec 2;21(1):137. doi: 10.1186/s10194-020-01208-0. No abstract available.
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PMID: 35410119BACKGROUNDEvers S, Afra J, Frese A, Goadsby PJ, Linde M, May A, Sandor PS; European Federation of Neurological Societies. EFNS guideline on the drug treatment of migraine--revised report of an EFNS task force. Eur J Neurol. 2009 Sep;16(9):968-81. doi: 10.1111/j.1468-1331.2009.02748.x.
PMID: 19708964BACKGROUNDLangohr HD, Gerber WD, Koletzki E, Mayer K, Schroth G. Clomipramine and metoprolol in migraine prophylaxis--a double-blind crossover study. Headache. 1985 Mar;25(2):107-13. doi: 10.1111/j.1526-4610.1985.hed2502107.x. No abstract available.
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PMID: 14982912BACKGROUNDBulut S, Berilgen MS, Baran A, Tekatas A, Atmaca M, Mungen B. Venlafaxine versus amitriptyline in the prophylactic treatment of migraine: randomized, double-blind, crossover study. Clin Neurol Neurosurg. 2004 Dec;107(1):44-8. doi: 10.1016/j.clineuro.2004.03.004.
PMID: 15567552BACKGROUNDCouch JR; Amitriptyline Versus Placebo Study Group. Amitriptyline in the prophylactic treatment of migraine and chronic daily headache. Headache. 2011 Jan;51(1):33-51. doi: 10.1111/j.1526-4610.2010.01800.x. Epub 2010 Nov 10.
PMID: 21070231BACKGROUNDSacco S, Bendtsen L, Ashina M, Reuter U, Terwindt G, Mitsikostas DD, Martelletti P. Correction to: European headache federation guideline on the use of monoclonal antibodies acting on the calcitonin gene related peptide or its receptor for migraine prevention. J Headache Pain. 2019 May 23;20(1):58. doi: 10.1186/s10194-019-0972-5.
PMID: 31122188BACKGROUNDKatsarava Z, Mania M, Lampl C, Herberhold J, Steiner TJ. Poor medical care for people with migraine in Europe - evidence from the Eurolight study. J Headache Pain. 2018 Feb 1;19(1):10. doi: 10.1186/s10194-018-0839-1.
PMID: 29392600BACKGROUNDBuettner C, Nir RR, Bertisch SM, Bernstein C, Schain A, Mittleman MA, Burstein R. Simvastatin and vitamin D for migraine prevention: A randomized, controlled trial. Ann Neurol. 2015 Dec;78(6):970-81. doi: 10.1002/ana.24534. Epub 2015 Nov 13.
PMID: 26418341BACKGROUNDHesami O, Sistanizad M, Asadollahzade E, Johari MS, Beladi-Moghadam N, Mazhabdar-Ghashghai H. Comparing the Effects of Atorvastatin With Sodium Valproate (Divalproex) on Frequency and Intensity of Frequent Migraine Headaches: A Double-blind Randomized Controlled Study. Clin Neuropharmacol. 2018 May/Jun;41(3):94-97. doi: 10.1097/WNF.0000000000000280.
PMID: 29746282BACKGROUNDGanji R, Majdinasab N, Hesam S, Rostami N, Sayyah M, Sahebnasagh A. Does atorvastatin have augmentative effects with sodium valproate in prevention of migraine with aura attacks? A triple-blind controlled clinical trial. J Pharm Health Care Sci. 2021 Apr 1;7(1):12. doi: 10.1186/s40780-021-00198-8.
PMID: 33789774BACKGROUNDSherafat A, Sahebnasagh A, Rahmany R, Mohammadi F, Saghafi F. The preventive effect of the combination of atorvastatin and nortriptyline in migraine-type headache: a randomized, triple-blind, placebo-controlled trial. Neurol Res. 2022 Apr;44(4):311-317. doi: 10.1080/01616412.2021.1981105. Epub 2022 Jan 17.
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PMID: 31881823BACKGROUND
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Marte-Helene Bjørk, Professor
Haukeland University Hospital
- PRINCIPAL INVESTIGATOR
Kjersti G. Vetvik, Ph.d.
University Hospital, Akershus
- PRINCIPAL INVESTIGATOR
Bendik S. Winswold, Post.doc.
Oslo University Hospital, UllevĂ¥l
- PRINCIPAL INVESTIGATOR
Anne H. Aamodt, Senior researcher
Oslo University Hospital
- PRINCIPAL INVESTIGATOR
Linn H Steffensen, Associate Professor II
University Hospital Northern Norway
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Masking Details
- Triple blind (blinded to patients, study personnel, and statistician)
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 10, 2024
First Posted
July 3, 2024
Study Start
May 1, 2024
Primary Completion (Estimated)
December 31, 2028
Study Completion (Estimated)
February 28, 2029
Last Updated
July 1, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share